电解质
材料科学
离子电导率
电化学
硫化物
化学工程
锂(药物)
纳米技术
制作
电导率
电流密度
锂电池
离子键合
电池(电)
硫化镍
离子液体
粘附
磷酸铁锂
电镀
膜
锂离子电池
无机化学
超级电容器
作者
Wanqing Jia,Jiayi Liu,Shiyu Yao,Xiaokong Liu,Fei Du
出处
期刊:
[American Chemical Society]
日期:2026-03-01
卷期号:3 (3): 418-427
被引量:5
摘要
High Resolution Image Download MS PowerPoint Slide The commercialization of all-solid-state lithium batteries (ASSLBs) is hindered by the lack of advanced binders for sulfide solid-state electrolyte (SSE) films, as current binders often fail to achieve cohesion and adhesion balance, resulting in agglomeration or insufficient mechanical strength. Herein, we introduce a self-healable supramolecular poly(urethane-urea) (SPU) binder for sulfide SSE films, leveraging dynamic hydrogen bonds to achieve a balance between adhesion and cohesion. The SPU binder enables the fabrication of free-standing Li 6 PS 5 Cl (LPSCl) films at a low binder content of 3 wt %, achieving an ionic conductivity of 1.5 mS cm –1 and a highly densified morphology. The resulting lithium symmetric cell exhibits a critical current density (CCD) of 1.8 mA cm –2 and cycling stability over 3500 h at 0.1 mA cm –2, and lithium dendrite growth is revealed to be largely mitigated in the LPSCl film. Furthermore, ASSLBs incorporating SPU-bound LPSCl films demonstrate enhanced rate capability (140.6 mAh g –1 at 1C) and cycling performance (78.8% capacity retention after 400 cycles). This work highlights the potential of self-healable binders in addressing the mechanical and electrochemical challenges of sulfide SSE films, paving the way for scalable ASSLB development.
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